Hypermobility Syndrome, 1st Edition

Diagnosis and Management for Physiotherapists
Authors :
Rosemary J. Keer & Rodney Grahame
Hypermobility syndrome (HMS) is an inherited connective tissue disorder affecting collagen that is characterized by a collection of features and symptoms. HMS is often encountered in patients, but it is easily overlooked. This practical resource educ ...view more
Hypermobility syndrome (HMS) is an inherited connective tissue disorder affecting collagen that is characterized by a collection of features and symptoms. HMS is often encountered in patients, but it is easily overlooked. This practical resource educates readers to its presentation, what to look for, and how best to treat it. Following a brief description of the historical and genetic background of the condition, HMS is described in relation to other connective tissue disorders, such as Ehlers-Danlos syndrome and the Marfan syndrome. Since HMS may occur in childhood, adolescence, adulthood, pregnancy, or old age, each of these stages is covered in the book, with detailed information on the presentation of the condition and its management.
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Hypermobility syndrome (HMS) is an inherited connective tissue disorder affecting collagen that is characterized by a collection of features and symptoms. HMS is often encountered in patients, but it is easily overlooked. This practical resource educates readers to its presentation, what to look for, and how best to treat it. Following a brief description of the historical and genetic background of the condition, HMS is described in relation to other connective tissue disorders, such as Ehlers-Danlos syndrome and the Marfan syndrome. Since HMS may occur in childhood, adolescence, adulthood, pregnancy, or old age, each of these stages is covered in the book, with detailed information on the presentation of the condition and its management.

Key Features
  • Demonstrates how to identify the condition in the clinic.
  • Discusses treatment and management strategies.
  • Provides examples in the form of case studies.
  • Includes details of a comprehensive assessment procedure, which differs depending on the stage of the disorder and the age of the patient.
  • Features contributions by experts in a range of medical fields.

Author Information
By Rosemary Keer, MSc, MCSP, MACP, SRP, Central London Physiotherapy Clinic, London, UK; and Rodney Grahame, CBE, MD, FRCP, FACP, Centre for Rheumatology, University College Hospitals London, London, UK